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PNPLA3

靶点ID:TCMBANKGE008368

靶点别名:ADPN; C22orf20; iPLA(2)epsilon

靶点描述:patatin like phospholipase domain containing 3

染色体:22

染色体位置:22q13.31

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:18590

OMIM_Link:609567

Ensembl_Link:ENSG00000100344

靶点对应的植物

ID	拉丁名	药名	药用植物名	功能与主治	来源	药用部位	使用民族

靶点对应的化合物

化合物ID	化合物名	别名	分子式	分子质量	Smiles

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000035	Digestive System Diseases; Infections	-	Disease or Syndrome	disease
TCMBANKDI000064	Digestive System Diseases	-	Disease or Syndrome	group
TCMBANKDI001779	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI003248	Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI007362	Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI008305	Digestive System Diseases; Infections	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	group
TCMBANKDI009278	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI011557	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI012932	Infections; Immune System Diseases	-	Disease or Syndrome	group
TCMBANKDI017769	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease
TCMBANKDI018048	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities	-	Disease or Syndrome	disease
TCMBANKDI018731	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI019962	Infections; Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	group
TCMBANKDI021455	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease
TCMBANKDI022322	-	-	Disease or Syndrome	disease
TCMBANKDI025194	-	-	Finding	disease
TCMBANKDI025502	-	-	Laboratory Procedure	phenotype
TCMBANKDI027906	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI030530	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	-	Sign or Symptom	phenotype
TCMBANKDI032496	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI032498	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease